Results 111 to 120 of about 18,247 (232)

Scleroderma in South Australia: epidemiological observations of possible pathogenic significance.

open access: yes, 2001
BACKGROUND: Scleroderma is an autoimmune disorder of unknown cause. Previous epidemiological studies have suggested some regional clustering and associations with occupations involving exposure to silica dusts and hydrocarbons.
Kencana Dharmapatni, AA   +15 more
core   +1 more source

Ocular Manifestation in Systemic Sclerosis—A Literature Review

open access: yesLife
Systemic sclerosis (SSc) is a chronic autoimmune connective tissue disease that affects more than 2 million people worldwide. It manifests through vasculopathy, an abnormal immunological response, and fibrosis leading to dysfunction of the multiple ...
Katarzyna Paczwa   +4 more
doaj   +1 more source

Clinical improvement of salt-and-pepper skin changes in juvenile systemic sclerosis using mycophenolate mofetil after intravenous methylprednisolone: a 3-year follow-up

open access: yesImmunological Medicine
In adult systemic sclerosis (SSc), salt-and-pepper skin changes can be used to diagnose diffuse cutaneous SSc during the early stages. However, reports of juvenile SSc (JSSc) with salt-and-pepper skin changes are unavailable.
Daisuke Hironaka   +8 more
doaj   +1 more source

Summary of Reported Cases of Nodular Scleroderma

open access: yes
Nodular (keloidal) Scleroderma (NS) constitutes a rare manifestation of cutaneous scleroderma, occurring either in conjunction with diffuse systemic sclerosis or as a localized form (morphea). The table summarizes the total number of NS cases reported in
Ntiri, M (via Mendeley Data)
core   +1 more source

A cross-sectional comparison of three self-reported functional indices in scleroderma

open access: yes, 2003
Objectives. In scleroderma, outcome measures such as skin score provide only limited information about the functional impact of the disease. The requirement for validated and convenient instruments that reliably reflect disease morbidity is now ...
Black, C. M.   +5 more
core   +1 more source

Scleroderma, a sign of aging

open access: yes, 2017
Hutchinson-Gilford progeria syndrome (HGPS) is regarded as a model for aging. Moreover, the mutant protein accumulating in progeria is to some extent also found in healthy aged individuals.
Verstraeten, V. L.R.M.
core   +1 more source

Non-cirrhotic Idiopathic portal hypertension in systemic sclerosis patients: report of one case and a systematic review of previous case reports

open access: yesAdvances in Rheumatology
Background The overlap of non-cirrhotic idiopathic portal hypertension (NCIPH) and systemic sclerosis (SSc) is rare. This article reports one case of a patient with SSc developing NCIPH and presents a systematic review of previously reported cases ...
Felipe Souza da Silva   +8 more
doaj   +1 more source

Are we ready to predict progressive disease in juvenile systemic sclerosis? [PDF]

open access: yesJ Scleroderma Relat Disord
Foeldvari I, Klotsche J, Torok KS.
europepmc   +1 more source

Diffuse fasciitis with eosinophilia. A clinicopathologic study

open access: yes, 1980
Three cases of diffuse fasciitis with eosinophilia are presented, and their clinical, laboratory and histologic follow-up are outlined. Furthermore histologic comparison with scleroderma is attempted and the literature is reviewed.
Shulman, L. E.   +5 more
core  

Pruritus associated with systemic sclerosis: a systematic review of treatment-based clinical trials. [PDF]

open access: yesRheumatol Int
Mortezaei K   +9 more
europepmc   +1 more source

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